Senior Manager EHS
View: 106
Update day: 06-05-2024
Location: Panjim / Panaji Goa
Category: Pharmaceutical / Chemical / Biotech Health / Medical Care Pharmacist / Pharmaceutical representatives
Industry: Pharmaceutical & Life Sciences
Position: Environment-Health-Safety
Job type: Full Time, Permanent
Experience: 15 - 24 years
Job content
Experience
15-20 Years
Min 3-5 years in Head EHS position for large size unit/multiple units
Qualification
B.Tech / Diploma in Chemical Engineering or MSC in Chemistry/Environment
Diploma in Industrial Safety is must
Certified safety officer from Goa Factory Inspectorate
Responsibilities
- Implementation of new EHS initiatives at all units at Goa
- EHS legal compliance monitoring and assurance prepare legal register as per state / central rules, implement system to follow all identified requirements
- Implement measures to ensure zero accident at both units and zero legal deviations
- Implementation of EHS system to ensure smooth ETP operation
- EHS training - Identify training needs, implement training system to ensure training as per the needs identified - training target (hours / days) compliance
- Periodic review and audits
- Implementation of EHS systems, SOPs and documents
- Monitor and ensure legal compliance related to air, water, Factories Act, etc.
- Ensure waste reduction measure implementation
- Implementation of EHS practices at both units to reduce unsafe acts /conditions and avoid accidents
- Implement initiatives to improve EHS culture at both units
- Implement process safety measures, change management
- Identify legal gaps, implement action plan to close the gaps
- Ensure on time submission of the legal forms / returns as per requirement
- Liasioning with government authorities, local village panchayats, etc.
Key Skills and Competencies
- Hands on experience in process safety, effluent treatment system operations, plant safety operation
- Hands on experience in handling the EHS department and related functions
- Good technical exposure / knowledge / understanding in pharmaceutical Industry. From good rated regulatory environment Industry
- Regulatory exposure of audits - USFDA, MHRA, EU, ANVISA, TGA etc.
- Very good communication (written and oral) and interpersonal skills
- Ability to work in a fast paced, demanding, timeline-driven environment
- Good analytical and problem-solving skills
- Listening, integrating diverse perspectives and add value to the achievement of team goals
- Ability to work independently and in team environment
- Ability to take initiatives and proactively seek quality solutions through emphasis on continuous improvement
- Hard working and honest
Deadline: 20-06-2024
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